nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Acyclic nucleoside phosphonates with a branched 2-(2-phosphonoethoxy)ethyl chain: Efficient synthesis and antiviral activity
|
Hocková, Dana |
|
2011 |
19 |
15 |
p. 4445-4453 9 p. |
artikel |
2 |
Analogue-based design, synthesis and molecular docking analysis of 2,3-diaryl quinazolinones as non-ulcerogenic anti-inflammatory agents
|
Manivannan, E. |
|
2011 |
19 |
15 |
p. 4520-4528 9 p. |
artikel |
3 |
Arthrinins A–D: Novel diterpenoids and further constituents from the sponge derived fungus Arthrinium sp.
|
Ebada, Sherif S. |
|
2011 |
19 |
15 |
p. 4644-4651 8 p. |
artikel |
4 |
Chemistry of ecteinascidins. Part 3: Preparation of 2′-N-acyl derivatives of ecteinascidin 770 and evaluation of cytotoxicity
|
Saktrakulkla, Panithi |
|
2011 |
19 |
15 |
p. 4421-4436 16 p. |
artikel |
5 |
Construction of dopamine sensors by using fluorescent ribonucleopeptide complexes
|
Liew, Fong Fong |
|
2011 |
19 |
15 |
p. 4473-4481 9 p. |
artikel |
6 |
Design, syntheses, and kinetic evaluation of 3-(phenylamino)oxazolidine-2,4-diones as potent cytochrome bc 1 complex inhibitors
|
Wang, Fu |
|
2011 |
19 |
15 |
p. 4608-4615 8 p. |
artikel |
7 |
Design, synthesis and biological evaluation of tyrosine-based hydroxamic acid analogs as novel histone deacetylases (HDACs) inhibitors
|
Zhang, Yingjie |
|
2011 |
19 |
15 |
p. 4437-4444 8 p. |
artikel |
8 |
Design, synthesis and biological evaluation of urea derivatives from o-hydroxybenzylamines and phenylisocyanate as potential FabH inhibitors
|
Li, Zi-Lin |
|
2011 |
19 |
15 |
p. 4413-4420 8 p. |
artikel |
9 |
Design, synthesis and evaluation of N-benzoylindazole derivatives and analogues as inhibitors of human neutrophil elastase
|
Crocetti, Letizia |
|
2011 |
19 |
15 |
p. 4460-4472 13 p. |
artikel |
10 |
Development of 3-substituted-androsterone derivatives as potent inhibitors of 17β-hydroxysteroid dehydrogenase type 3
|
Maltais, René |
|
2011 |
19 |
15 |
p. 4652-4668 17 p. |
artikel |
11 |
Discovery of benzimidazole derivatives as novel multi-target EGFR, VEGFR-2 and PDGFR kinase inhibitors
|
Li, Yunqi |
|
2011 |
19 |
15 |
p. 4529-4535 7 p. |
artikel |
12 |
Discovery of potent, selective, and orally bioavailable quinoline-based dipeptidyl peptidase IV inhibitors targeting Lys554
|
Maezaki, Hironobu |
|
2011 |
19 |
15 |
p. 4482-4498 17 p. |
artikel |
13 |
Discovery of selective indole-based prostaglandin D2 receptor antagonist
|
Iwahashi, Maki |
|
2011 |
19 |
15 |
p. 4574-4588 15 p. |
artikel |
14 |
Discovery of vinylogous carbamates as a novel class of β-ketoacyl-acyl carrier protein synthase III (FabH) inhibitors
|
Li, Huan-Qiu |
|
2011 |
19 |
15 |
p. 4454-4459 6 p. |
artikel |
15 |
Editorial board
|
|
|
2011 |
19 |
15 |
p. IFC- 1 p. |
artikel |
16 |
Fragmental modeling of hPepT2 and analysis of its binding features by docking studies and pharmacophore mapping
|
Pedretti, Alessandro |
|
2011 |
19 |
15 |
p. 4544-4551 8 p. |
artikel |
17 |
Graphical contents list
|
|
|
2011 |
19 |
15 |
p. 4405-4412 8 p. |
artikel |
18 |
Human HDAC isoform selectivity achieved via exploitation of the acetate release channel with structurally unique small molecule inhibitors
|
Whitehead, Lewis |
|
2011 |
19 |
15 |
p. 4626-4634 9 p. |
artikel |
19 |
Molecular factors governing inhibition of arylimidamides against Leishmania: Conservative computational modeling to improve chemotherapies
|
Collar, Catharine J. |
|
2011 |
19 |
15 |
p. 4552-4561 10 p. |
artikel |
20 |
Requirements for mammalian carboxylesterase inhibition by substituted ethane-1,2-diones
|
Parkinson, Elizabeth I. |
|
2011 |
19 |
15 |
p. 4635-4643 9 p. |
artikel |
21 |
Synthesis and antimalarial activity of new heterocyclic hybrids based on chloroquine and thiazolidinone scaffolds
|
Rojas Ruiz, Fernando A. |
|
2011 |
19 |
15 |
p. 4562-4573 12 p. |
artikel |
22 |
Synthesis and antiviral evaluation of 9-(S)-[3-alkoxy-2-(phosphonomethoxy)propyl]nucleoside alkoxyalkyl esters: Inhibitors of hepatitis C virus and HIV-1 replication
|
Valiaeva, Nadejda |
|
2011 |
19 |
15 |
p. 4616-4625 10 p. |
artikel |
23 |
Synthesis and biological activity of naphthyl-substituted (B-ring) benzophenone derivatives as novel non-nucleoside HIV-1 reverse transcriptase inhibitors
|
Ma, Xiao-Dong |
|
2011 |
19 |
15 |
p. 4601-4607 7 p. |
artikel |
24 |
Synthesis and biological evaluation of 4β-acrylamidopodophyllotoxin congeners as DNA damaging agents
|
Kamal, Ahmed |
|
2011 |
19 |
15 |
p. 4589-4600 12 p. |
artikel |
25 |
Synthesis and SERCA activities of structurally simplified cyclopiazonic acid analogues
|
Yao, Sheng |
|
2011 |
19 |
15 |
p. 4669-4678 10 p. |
artikel |
26 |
Synthesis, in vitro and in vivo evaluation of fluorine-18 labelled FE-GW405833 as a PET tracer for type 2 cannabinoid receptor imaging
|
Evens, Nele |
|
2011 |
19 |
15 |
p. 4499-4505 7 p. |
artikel |
27 |
Synthesis, molecular modeling and biological evaluation of β-ketoacyl-acyl carrier protein synthase III (FabH) as novel antibacterial agents
|
Zhang, Hong-Jia |
|
2011 |
19 |
15 |
p. 4513-4519 7 p. |
artikel |
28 |
Synthesis of some new [1,2,4]triazolo[3,4-b][1,3,4]thiadiazines and [1,2,4]triazolo[3,4-b][1,3,4] thiadiazoles starting from 5-nitro-2-furoic acid and evaluation of their antimicrobial activity
|
Badr, Sahar M.I. |
|
2011 |
19 |
15 |
p. 4506-4512 7 p. |
artikel |
29 |
Understanding non-enzymatic aminophospholipid glycation and its inhibition. Polar head features affect the kinetics of Schiff base formation
|
Caldés, Catalina |
|
2011 |
19 |
15 |
p. 4536-4543 8 p. |
artikel |